3-甲基喹啉
3-甲基喹啉结构式
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常用名 | 3-甲基喹啉 | 英文名 | 3-Methylquinoline |
|---|---|---|---|---|
| CAS号 | 612-58-8 | 分子量 | 143.185 | |
| 密度 | 1.1±0.1 g/cm3 | 沸点 | 259.8±0.0 °C at 760 mmHg | |
| 分子式 | C10H9N | 熔点 | 16-17 °C(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 104.9±11.3 °C | |
| 符号 |
GHS05, GHS07, GHS08 |
信号词 | Danger |
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Time-of-flight accurate mass spectrometry identification of quinoline alkaloids in honey.
Anal. Bioanal. Chem 407 , 6159-70, (2015) Time-of-flight accurate mass spectrometry (TOF-MS), following a previous chromatographic (gas or liquid chromatography) separation step, is applied to the identification and structural elucidation of quinoline-like alkaloids in honey. Both electron ionization... |
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Tetra-μ-benzoato-bis-[(3-methyl-quinoline)copper(II)](Cu-Cu).
Acta Crystallogr. Sect. E Struct. Rep. Online 64(9) , m1141, (2008) In the title compound, [Cu(2)(C(7)H(5)O(2))(4)(C(10)H(9)N)(2)], the paddle-wheel-type dinuclear complex mol-ecule contains four bridging benzoate groups and two terminal 3-methyl-quinoline ligands. The asymmetric unit contains one and a half mol-ecules with a... |
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Microbial metabolism of quinoline and related compounds. XVII. Degradation of 3-methylquinoline by Comamonas testosteroni 63.
Biol. Chem. Hoppe-Seyler 374(3) , 175-81, (1993) A bacterial strain which utilizes 3-methylquinoline as sole source of carbon, nitrogen and energy was isolated from activated sludge. On the basis of its morphological and physiological characteristics, this isolate was classified as Comamonas testosteroni. F... |
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Quinoline 2-oxidoreductase and 2-oxo-1,2-dihydroquinoline 5,6-dioxygenase from Comamonas testosteroni 63. The first two enzymes in quinoline and 3-methylquinoline degradation.
Eur. J. Biochem. 232(2) , 536-44, (1995) The enzymes catalysing the first two steps of quinoline and 3-methylquinoline degradation by Comamonas testosteroni 63 were investigated. Quinoline 2-oxidoreductase, which catalyses the hydroxylation of (3-methyl-)quinoline to (3-methyl-)2-oxo-1,2-dihydroquin... |
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Selective synthesis of 2-methylquinoline over zeolites. Reddy PR, et al.
Catal. Letters 56(2-3) , 155-58, (1998)
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